WO2009105024A1 - Multilayered coated cutting tool - Google Patents

Multilayered coated cutting tool Download PDF

Info

Publication number
WO2009105024A1
WO2009105024A1 PCT/SE2009/050185 SE2009050185W WO2009105024A1 WO 2009105024 A1 WO2009105024 A1 WO 2009105024A1 SE 2009050185 W SE2009050185 W SE 2009050185W WO 2009105024 A1 WO2009105024 A1 WO 2009105024A1
Authority
WO
WIPO (PCT)
Prior art keywords
men
cutting tool
cubic
tool according
layers
Prior art date
Application number
PCT/SE2009/050185
Other languages
French (fr)
Inventor
Mats Johansson
Jacob Sjölén
Magnus ODÉN
Axel Knutsson
Original Assignee
Seco Tools Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Seco Tools Ab filed Critical Seco Tools Ab
Priority to EP09711935.8A priority Critical patent/EP2247772B1/en
Priority to CN200980106128.3A priority patent/CN101952482B/en
Priority to US12/867,889 priority patent/US8409696B2/en
Publication of WO2009105024A1 publication Critical patent/WO2009105024A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/06Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/52Multiple coating or impregnating multiple coating or impregnating with the same composition or with compositions only differing in the concentration of the constituents, is classified as single coating or impregnation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23BTURNING; BORING
    • B23B27/00Tools for turning or boring machines; Tools of a similar kind in general; Accessories therefor
    • B23B27/14Cutting tools of which the bits or tips or cutting inserts are of special material
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/009After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/80After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics
    • C04B41/81Coating or impregnation
    • C04B41/85Coating or impregnation with inorganic materials
    • C04B41/87Ceramics
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/80After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics
    • C04B41/81Coating or impregnation
    • C04B41/89Coating or impregnation for obtaining at least two superposed coatings having different compositions
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/0021Reactive sputtering or evaporation
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/06Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • C23C14/0641Nitrides
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/22Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
    • C23C14/24Vacuum evaporation
    • C23C14/32Vacuum evaporation by explosion; by evaporation and subsequent ionisation of the vapours, e.g. ion-plating
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C30/00Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
    • C23C30/005Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process on hard metal substrates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23BTURNING; BORING
    • B23B2222/00Materials of tools or workpieces composed of metals, alloys or metal matrices
    • B23B2222/36Nickel chrome alloys, e.g. Inconel®
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23BTURNING; BORING
    • B23B2222/00Materials of tools or workpieces composed of metals, alloys or metal matrices
    • B23B2222/80Stainless steel
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23BTURNING; BORING
    • B23B2224/00Materials of tools or workpieces composed of a compound including a metal
    • B23B2224/24Titanium aluminium nitride
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23BTURNING; BORING
    • B23B2228/00Properties of materials of tools or workpieces, materials of tools or workpieces applied in a specific manner
    • B23B2228/08Properties of materials of tools or workpieces, materials of tools or workpieces applied in a specific manner applied by physical vapour deposition [PVD]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24942Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
    • Y10T428/2495Thickness [relative or absolute]
    • Y10T428/24967Absolute thicknesses specified
    • Y10T428/24975No layer or component greater than 5 mils thick
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/26Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
    • Y10T428/263Coating layer not in excess of 5 mils thick or equivalent
    • Y10T428/264Up to 3 mils
    • Y10T428/2651 mil or less

Definitions

  • the present invention relates to a tool for machining by chip removal comprising a body of a hard alloy of cemented carbide, cermet, ceramics, cubic boron nitride based material or high speed steel and a hard and wear resistant metal nitride coating comprising alternating cubic structured (Ti,Al)N layers and cubic structured MeN layers, where Me is one or more of the metal elements Ti, Zr, Hf, V, Nb, Ta, Mo and Al.
  • the coating is grown by physical vapour deposition (PVD) and preferably by cathodic arc evaporation.
  • PVD physical vapour deposition
  • This invention is particularly useful in metal cutting applications generating high temperatures, e.g., machining of super alloys and stainless steel.
  • Coating optimization has also been obtained by applying different concepts of multilayer as; alternating Ti and Al containing layers (US 6,309,738), oxygen and non- oxygen containing layers (US 6,254,984), one of the layers stacked in the multilayer consists itself of a multilayer (US 6,077,596), alternating nitrogen content (US 5,330,853) or using one metastable compound (US 5,503,912) or as aperiodic multilayer (US 6,103,357).
  • JP 6136514 discloses a wear resistant multilayered hard coating structure comprising alternating layers of Ti(C, N) and (Al, Ti)(C, N) on the surface of the tool.
  • the coating is deposited by PVD at a relatively low temperature.
  • the coating hardens as a nanocomposite, adapting its strength during spinodal decomposition of (Ti Al)N in cubic TiN and cubic AlN domains where the additional MeN layers provide means for locking a predominantly overall cubic coating structure (as measured by X-ray diffraction) thus suppressing the detrimental hexagonal AlN phase formation otherwise occurring.
  • Fig Ia Schematic coating structure showing (1) body, (2) multilayer coating, (3) MeN layer, (4) (Ti, Al)N layer and (5) the repeat period ⁇ .
  • Fig Ib Schematic coating structure showing (1) body, (2) inner single- and/or multilayer coating according to prior art, (3) multilayer coating according to the invention and (4) outer single- and/or multilayer coating according to prior art.
  • Fig 2a Schematic view (side view) of the deposition chamber showing (1) vacuum chamber, (2a) cathode material A, (2b) cathode material B, (3) fixture, (4) power supply for biasing, (5a) cathodic arc power supply (5b) cathodic arc power supply, (6) inlet for process gas and (7) outlet for vacuum pump.
  • Fig 2b Schematic view (top view) of the deposition chamber showing (1) vacuum chamber, (2) four positions for different cathode materials and (3) fixture.
  • FIG. 1 (A) Cross sectional STEM micrograph of a coating with TiN (bright contrast) and (Ti 5 Al)N (dark contrast) and (B) schematic representation of the grain structure of a typical multilayer coating according to this invention.
  • Fig 4 X-ray diffraction patterns obtained from (A) a pure (Ti 5 Al)N layer and (B) multilayer TiNZ(Ti 5 Al)N coating according to the invention.
  • the diffraction peaks are indexed as (1) TiN, (2) (TiAl)N and (3) cemented carbide.
  • a cutting tool for machining by chip removal comprising a body of a hard alloy of cemented carbide, cermet, ceramics, cubic boron nitride based material or high speed steel on which a hard and wear resistant coating is applied comprising a polycrystalline laminar, multilayered structure of metal nitride compounds, in a repetitive form (see Fig. Ia) ...MeN(3)/(Ti). x Al x )N(4)/MeN(3)/(Ti, -x Al x )N(4)/MeN(3)/(Ti, -x Al x )N(4)/MeN(3)/...
  • Said laminar structure has a total thickness of 0.5 to 20 ⁇ m, preferably 1 to 10 ⁇ m and most preferably 2 to 5 ⁇ m.
  • the repeat period ⁇ , (5) in Fig. Ia i.e., the total thickness of the bi-layer d Me N + df T j ;A i)N 5 is essentially constant throughout the entire multi layer structure (that is, it varies by no more than 20 %).
  • the repeat period is 5 nm ⁇ ⁇ 20 nm, preferably 5 nm ⁇ ⁇ 10 nm with 1/10 ⁇ (d Me N /d( ⁇ i, A i)N) ⁇ 1/3 and where the thickness d MeN is larger than d MeN ⁇ l nm.
  • Me is Ti
  • Me is Zr. In a third embodiment Me is V.
  • Me is Nb.
  • Me is Ta.
  • Me is Al.
  • Me is two or more of the metal elements Ti, V, Nb or Al.
  • Me is two or more of the metal elements V, Nb or Al.
  • Me is two or more of the metal elements Ti, Zr, V or Nb.
  • Me is two or more of the metal elements Zr, V or Nb.
  • Said body (1) in fig Ib may be coated with an inner (3) single- and/or multilayer coating of TiN, TiC, Ti(C 5 N) or (Ti 5 Al)N, preferably (Ti 5 Al)N and/or an outer (4) single- and/or multilayer coating of TiN, TiC 5 Ti(C 5 N) or (Ti 5 Al)N, preferably (Ti 5 Al)N, to a total coating thickness 1 to 20 ⁇ m, preferably 1 to 10 ⁇ m and most preferably 2 to 7 ⁇ m according to prior art.
  • the MeN layer has a compressive stress level between -12.0 ⁇ ⁇ (MeN) ⁇ -3.0 GPa 5 preferably between - 12.0 ⁇ ⁇ (MeN) ⁇ -8.0 GPa whereas the (Ti, -X A1 X )N layer has a stress level varying between -6.0 ⁇ ⁇ ((Ti 1-x Al x )N) ⁇ -0.5 GPa, preferably between -6.0 ⁇ ⁇ ((Ti, -x Al x )N) ⁇ -3.0 GPa.
  • the average composition of the MeNZ(Ti 1 -X A1 X )N multilayer coating is 46 at% ⁇ Zr + Hf + V +Nb + Ta + Mo + Ti + Al ⁇ 54 at%, preferably 48 at% ⁇ Zr + Hf + V +Nb + Ta + Mo + Ti + Al ⁇ 52 at% and balanced N.
  • the coating process of the present invention is based on cathodic arc evaporation of pure and/or alloyed cathodes under the following conditions; (Ti] -X A1 X )N layers are grown using Ti/Al-cathodes with a composition between (70 at% Ti + 30 at% Al) and (5 at% Ti + 95 at% Al) and preferably between (40 at% Ti + 60 at% Al) and (30 at% Ti + 70 at% Al).
  • the MeN layers are grown using pure or alloyed cathodes where Me is one or more of the metal elements Ti, Zr, Hf, V, Nb, Ta, Mo and Al, preferably one or more of Ti, V, Nb, Ta or Al.
  • the evaporation current is between 50 A and 200 A depending on the cathode size and preferably between 50 A and 100 A using cathodes of 63 mm in diameter.
  • the layers are grown in an Ar + N 2 atmosphere, preferably in a pure N 2 atmosphere, at a total pressure of 0.5 Pa to 9.0 Pa, preferably 1.5 Pa to 5.0 Pa.
  • the bias is - 10 V to -300 V, preferably -20 V to - 100V.
  • the deposition temperature is between 350 0 C and 700 0 C, preferably between 400 0 C and 650 0 C.
  • the invention also relates to the use of cutting tool inserts according to the above for machining of stainless steel and super alloys at cutting speeds of 50-400 m/min, preferably 75-300 m/min, with an average feed, per tooth in the case of milling, of 0.08- 0.5 mm, preferably 0.1-0.4 mm depending on cutting speed and insert geometry.
  • Cemented carbide inserts with composition 94 wt% WC - 6 wt% Co (WC grain size of 0.8 ⁇ m) were used.
  • the inserts were cleaned in ultrasonic baths of an alkali solution and alcohol.
  • the system was evacuated to a pressure of less than 2.OxIO "3 Pa, after which the inserts were sputter cleaned with Ar ions.
  • TiNZ(Ti 1-x Al x )N layers were grown using cathodic arc evaporation.
  • the cathode materials for (Ti 1 ⁇ Al x )N was Ti/Al (33 at% Ti + 67 at% Al), 63 mm in diameter (position (2a) in fig 2a) and for the TiN layers, pure Ti (63 mm in diameter, position (2b) in fig 2a) was used.
  • the layers were deposited in 5 99.995% pure N 2 atmosphere at a total pressure of 4 Pa, using a bias of -40 V and an evaporation current of 6OA for both cathode materials.
  • the variation in layer thicknesses was obtained by altering the evaporation current to the cathodes, the set-up of the deposition system (i.e., the cathode material in the four positions (2), see fig 2b) and the rotation speed of the fixture (see tab 1).
  • the total coating thickness was close to 3 ⁇ m o for all inserts.
  • the deposition temperature was about 450 0 C.
  • TEM transmission electron microscopy
  • STEM scanning TEM
  • FE3 focused ion beam
  • Fig 4 shows XRD patterns of (A) single phase (Ti o,36 Alo .64 )N layer and (B) multilayered TiNZ(Ti 5 Al)N coating with TiN and (Ti 036 Al 064 )N.
  • the indexed peaks correspond to single phase (1) TiN, (2) (Ti 9 Al)N and 2 5 (3) cemented carbide.
  • all deposited coatings summarized in tab 1 reveal single-phase cubic TiN and (Ti 5 Al)N structures.
  • the residual stresses, ⁇ , of the TiN and (Ti i -x Al x )N layers of the coating were evaluated by XRD measurements (see tab 1 ) using the sin 2 ⁇ method.
  • the measurements were performed using CuK ⁇ -radiation on the TiN 220- and the (Ti i -x Al x )N 220- reflections, respectively. Stress values for layers thinner than ⁇ 4 nm could not be deduced.
  • the goniometer setup is shown in Fig. 5. Data was obtained using the side- inclination technique ( ⁇ -geometry) with 11 , ⁇ -angles (positive and negative), equidistant within a sin 2 ⁇ range of 0 to 0.82 ( ⁇ 65°).
  • the total average composition of the coatings was estimated by energy dispersive spectroscopy (EDS) analysis area using a LEO Ultra 55 scanning electron microscope with a Thermo Noran EDS detector operating at 10 kV.
  • the data were evaluated using a Noran System Six (NSS ver 2) software (see tab 1).
  • NSS ver 2 Noran System Six
  • Example 1 was repeated but using a pure Ta cathode (63mm in diameter, position (2b) in fig 2a) for growth of the TaN layers.
  • the total average composition of the coatings was estimated by energy dispersive spectroscopy (EDS) analysis (see example 1) and summarized in tab 2.
  • EDS energy dispersive spectroscopy
  • Example 1 was repeated but using a Ti/Nb (95at%Ti + 5at% Nb) cathode (63 mm in diameter, position (2b) in fig 2a) for growth of the (Ti 5 Nb)N layers.
  • Example 1 was repeated but using a pure Nb cathode (63 mm in diameter, position (2b) in fig 2a) for growth of the NbN layers.
  • Example 1 was repeated but using a pure Zr cathode (63mm in diameter, position (2b) in fig 2a) for growth of the ZrN layers.
  • the total average composition of the coatings was estimated by energy dispersive spectroscopy (EDS) analysis (see example 1) and summarized in tab 5.
  • EDS energy dispersive spectroscopy
  • Example 2 was repeated but using a pure V cathode (63 mm in diameter, position (2b) in fig 2a) for growth of the VN layers.
  • Example 2 was repeated but using a Al/Ti (95at%Al + 5at% Ti) cathode (63mm in diameter, position (2b) in fig 2a) for growth of the (Al 5 Ti)N layers.
  • the total average composition of the coatings was estimated by energy dispersive spectroscopy (EDS) analysis (see example 1) and summarized in tab 7.
  • EDS energy dispersive spectroscopy
  • FIG. 8 shows a STEM micrographs of the coating of sample 4 (Tab 1). The image shows TiN rich regions (brighter contrast) and AlN rich regions (darker contrast). This is further verified by the EDS mapping in (C) and (D) showing the EDS maps of Ti (bright areas show Ti rich regions) and Al (bright areas show Al rich regions), respectively. Further, the typical size of the Ti and Al rich regions is on the order of 5 nm.
  • Selected area electron diffraction patterns (B) show coherency and cubic structure over the layered structure.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Ceramic Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Metallurgy (AREA)
  • Structural Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Cutting Tools, Boring Holders, And Turrets (AREA)
  • Physical Vapour Deposition (AREA)

Abstract

The present invention relates to a cutting tool for the machining of stainless steel and super alloys comprising a body (1) of a hard alloy of cemented carbide, cermet, ceramics, cubic boron nitride based material or high speed steel and on which at least one of the functioning parts of the surface thereof, a hard and wear resistant coating is applied. The coating comprises a polycrystalline laminar, multilayered structure (2) of metal nitride compounds, in a repetitive form...MeN/( Ti1_xA1x)N /MeN/ ( Ti1-A1x)N /MeN/ (Ti1- xA1x)N/MeN/( Ti1_xA1x) N... of cubic structured (Ti1_xA1x)N layers where 0.3 < x < 0.95 and cubic structured MeN layers (3) where Me is one or more of the metal element Ti, Zr, Hf, V, Nb, Ta, Mo and Al. The laminated structure has a repeat period, λ (5), of 5 nm < λ < 20 nm, a layer thickness relation of 1/10 < (dMeN /d (Ti, A1) N) < 1/3 and a thickness dMeN ≥1 nm that is essentially constant throughout its total thickness up to 20 μm. The coating hardens as a nanocomposite, adapting its strength during spinodal decomposition of (Ti1_xA1x)N (4) in cubic TiN and cubic ALN domains where the additional cubic structured MeN layers provides means for locking a predominantly overall cubic coating structure thus suppressing the hexagonal ALN phase formation leading to improved high temperature metal cutting properties. The MeN layers are grown by cathodic arc evaporation.

Description

MULTILAYERED COATED CUTTING TOOL
BACKGROUND OF THE INVENTION
The present invention relates to a tool for machining by chip removal comprising a body of a hard alloy of cemented carbide, cermet, ceramics, cubic boron nitride based material or high speed steel and a hard and wear resistant metal nitride coating comprising alternating cubic structured (Ti,Al)N layers and cubic structured MeN layers, where Me is one or more of the metal elements Ti, Zr, Hf, V, Nb, Ta, Mo and Al. The coating is grown by physical vapour deposition (PVD) and preferably by cathodic arc evaporation. This invention is particularly useful in metal cutting applications generating high temperatures, e.g., machining of super alloys and stainless steel.
Since the early 1980's, TiN-layers have been widely used for surface protective applications. In order to improve the oxidation resistance of these coatings, work began in the mid- 1980's with adding aluminium to TiN [see e.g. H. A. Jehn, et al, J. Vac. Sci.
Technol. A 4, 2701 (1986) and O. Knotek et.al, J. Vac. Sci. Technol. A 4, 2695 (1986)].
The compound thus formed, cubic-phase (Ti Al)N, was found to have superior oxidation resistance and enabled greater cutting speeds during machining, prolonged tool life, machining of harder materials, and improved manufacturing economy. Improved coating performance in metal cutting applications has been obtained by precipitation hardening of (Ti5Al)N [see e.g. A. Hδrling et al, Surf. Coat. Tech. 191 (2005)] and also disclosed in US 7,083,868 and US 7,056,602.
Coating optimization has also been obtained by applying different concepts of multilayer as; alternating Ti and Al containing layers (US 6,309,738), oxygen and non- oxygen containing layers (US 6,254,984), one of the layers stacked in the multilayer consists itself of a multilayer (US 6,077,596), alternating nitrogen content (US 5,330,853) or using one metastable compound (US 5,503,912) or as aperiodic multilayer (US 6,103,357).
JP 6136514 discloses a wear resistant multilayered hard coating structure comprising alternating layers of Ti(C, N) and (Al, Ti)(C, N) on the surface of the tool. The coating is deposited by PVD at a relatively low temperature.
The trends towards dry- work processes for environmental protection, i.e., metal cutting operation without using cutting fluids (lubricants) and accelerated machining speed with improved process put even higher demands on the characteristics of the tool materials due to an increased tool cutting-edge temperature. In particular, coating stability at high temperatures, e.g., oxidation- and wear-resistance have become even more crucial.
It is an object of the present invention to provide a coated cutting tool yielding improved performance in metal cutting applications at elevated temperatures.
Surprisingly, we have found that by combining two different cubic structured materials in a multilayered coating leads to improved high temperature metal cutting properties. The coating hardens as a nanocomposite, adapting its strength during spinodal decomposition of (Ti Al)N in cubic TiN and cubic AlN domains where the additional MeN layers provide means for locking a predominantly overall cubic coating structure (as measured by X-ray diffraction) thus suppressing the detrimental hexagonal AlN phase formation otherwise occurring. BRIEF DESCRIPTION OF THE DRAWINGS
Fig Ia; Schematic coating structure showing (1) body, (2) multilayer coating, (3) MeN layer, (4) (Ti, Al)N layer and (5) the repeat period λ.
Fig Ib; Schematic coating structure showing (1) body, (2) inner single- and/or multilayer coating according to prior art, (3) multilayer coating according to the invention and (4) outer single- and/or multilayer coating according to prior art.
Fig 2a; Schematic view (side view) of the deposition chamber showing (1) vacuum chamber, (2a) cathode material A, (2b) cathode material B, (3) fixture, (4) power supply for biasing, (5a) cathodic arc power supply (5b) cathodic arc power supply, (6) inlet for process gas and (7) outlet for vacuum pump.
Fig 2b; Schematic view (top view) of the deposition chamber showing (1) vacuum chamber, (2) four positions for different cathode materials and (3) fixture.
Fig 3; (A) Cross sectional STEM micrograph of a coating with TiN (bright contrast) and (Ti5Al)N (dark contrast) and (B) schematic representation of the grain structure of a typical multilayer coating according to this invention.
Fig 4; X-ray diffraction patterns obtained from (A) a pure (Ti5Al)N layer and (B) multilayer TiNZ(Ti5Al)N coating according to the invention. The diffraction peaks are indexed as (1) TiN, (2) (TiAl)N and (3) cemented carbide. ig 5; Schematic of the set-up used for residual stress, σ, analysis by XRD Fig 6; STEM micrographs of a TiN/(Ti,Al)N multilayer coating of TiN (2 nm) and (Ti Al)N (7,9 nm) showing (A) the (Ti Al)N layer, (B) electron diffraction pattern over the region in (A), (C) Ti EDS map (bright contrast) and (D) Al EDS map (bright contrast).
DETAILED DESCRIPTION OF THE INVENTION
According to the present invention, there is provided a cutting tool for machining by chip removal comprising a body of a hard alloy of cemented carbide, cermet, ceramics, cubic boron nitride based material or high speed steel on which a hard and wear resistant coating is applied comprising a polycrystalline laminar, multilayered structure of metal nitride compounds, in a repetitive form (see Fig. Ia) ...MeN(3)/(Ti). xAlx)N(4)/MeN(3)/(Ti,-xAlx)N(4)/MeN(3)/(Ti,-xAlx)N(4)/MeN(3)/... of cubic structured (Ti1-XA1X)N layers 0.3 < x < 0.95, preferably 0.45 < x < 0.75 and cubic structured MeN layers where Me is one or more of the metal elements Ti, Zr, Hf, V, Nb, Ta, Mo and Al, preferably Ti, V, Nb, Ta and Al.
Said laminar structure has a total thickness of 0.5 to 20 μm, preferably 1 to 10 μm and most preferably 2 to 5 μm. The repeat period λ, (5) in Fig. Ia, i.e., the total thickness of the bi-layer dMeN + dfTj;Ai)N5 is essentially constant throughout the entire multi layer structure (that is, it varies by no more than 20 %). The repeat period is 5 nm < λ< 20 nm, preferably 5 nm < λ< 10 nm with 1/10 < (dMeN /d(τi,Ai)N) < 1/3 and where the thickness dMeN is larger than dMeN ≥l nm.
In a first embodiment Me is Ti.
In a second embodiment Me is Zr. In a third embodiment Me is V.
In a forth embodiment Me is Nb.
In a fifth embodiment Me is Ta.
In a sixth embodiment Me is Al.
In a seventh embodiment Me is two or more of the metal elements Ti, V, Nb or Al.
In an eighth embodiment Me is two or more of the metal elements V, Nb or Al.
In a ninth embodiment Me is two or more of the metal elements Ti, Zr, V or Nb.
In a tenth embodiment Me is two or more of the metal elements Zr, V or Nb.
Said body (1) in fig Ib may be coated with an inner (3) single- and/or multilayer coating of TiN, TiC, Ti(C5N) or (Ti5Al)N, preferably (Ti5Al)N and/or an outer (4) single- and/or multilayer coating of TiN, TiC5 Ti(C5N) or (Ti5Al)N, preferably (Ti5Al)N, to a total coating thickness 1 to 20 μm, preferably 1 to 10 μm and most preferably 2 to 7 μm according to prior art.
The MeN layer has a compressive stress level between -12.0 < σ(MeN) < -3.0 GPa5 preferably between - 12.0 < σ(MeN) < -8.0 GPa whereas the (Ti,-XA1X)N layer has a stress level varying between -6.0 < σ((Ti1-x Alx)N) < -0.5 GPa, preferably between -6.0 < σ((Ti,-xAlx)N) < -3.0 GPa.
SUBSTI rUTE SHEET (RULE 26) The average composition of the MeNZ(Ti1 -XA1X)N multilayer coating is 46 at% < Zr + Hf + V +Nb + Ta + Mo + Ti + Al < 54 at%, preferably 48 at% < Zr + Hf + V +Nb + Ta + Mo + Ti + Al < 52 at% and balanced N.
The coating process of the present invention is based on cathodic arc evaporation of pure and/or alloyed cathodes under the following conditions; (Ti]-XA1X)N layers are grown using Ti/Al-cathodes with a composition between (70 at% Ti + 30 at% Al) and (5 at% Ti + 95 at% Al) and preferably between (40 at% Ti + 60 at% Al) and (30 at% Ti + 70 at% Al). The MeN layers are grown using pure or alloyed cathodes where Me is one or more of the metal elements Ti, Zr, Hf, V, Nb, Ta, Mo and Al, preferably one or more of Ti, V, Nb, Ta or Al. The evaporation current is between 50 A and 200 A depending on the cathode size and preferably between 50 A and 100 A using cathodes of 63 mm in diameter. The layers are grown in an Ar + N2 atmosphere, preferably in a pure N2 atmosphere, at a total pressure of 0.5 Pa to 9.0 Pa, preferably 1.5 Pa to 5.0 Pa. The bias is - 10 V to -300 V, preferably -20 V to - 100V. The deposition temperature is between 350 0C and 700 0C, preferably between 400 0C and 650 0C.
The invention also relates to the use of cutting tool inserts according to the above for machining of stainless steel and super alloys at cutting speeds of 50-400 m/min, preferably 75-300 m/min, with an average feed, per tooth in the case of milling, of 0.08- 0.5 mm, preferably 0.1-0.4 mm depending on cutting speed and insert geometry.
Example 1
Cemented carbide inserts with composition 94 wt% WC - 6 wt% Co (WC grain size of 0.8 μm) were used.
Before deposition, the inserts were cleaned in ultrasonic baths of an alkali solution and alcohol. The system was evacuated to a pressure of less than 2.OxIO"3 Pa, after which the inserts were sputter cleaned with Ar ions. TiNZ(Ti 1-x Alx)N layers were grown using cathodic arc evaporation. The cathode materials for (Ti1^Alx)N was Ti/Al (33 at% Ti + 67 at% Al), 63 mm in diameter (position (2a) in fig 2a) and for the TiN layers, pure Ti (63 mm in diameter, position (2b) in fig 2a) was used. The layers were deposited in 5 99.995% pure N2 atmosphere at a total pressure of 4 Pa, using a bias of -40 V and an evaporation current of 6OA for both cathode materials. The variation in layer thicknesses was obtained by altering the evaporation current to the cathodes, the set-up of the deposition system (i.e., the cathode material in the four positions (2), see fig 2b) and the rotation speed of the fixture (see tab 1). The total coating thickness was close to 3 μm o for all inserts. The deposition temperature was about 450 0C.
Cross-sectional transmission electron microscopy (TEM) including scanning TEM (STEM) was used to study the microstructure of the layers. The sample preparation comprised standard mechanical grinding/polishing and ion-beam sputter ,5 etching on both upper and lower surfaces as well as cut-out of TEM samples by using focused ion beam (FE3) milling over the cutting edge of the inserts. Fig 3 (A) is a cross sectional STEM micrograph of a multilayer coating with TiN (bright contrast) and (Ti036Al064)N (dark contrast). The microstructure is columnar and dense, with large single crystal grains over several interfaces (schematically shown in (B)).
20
The XRD patterns of the as-deposited layers were obtained using Cu K alpha radiation and a Θ-2Θ configuration. Fig 4 shows XRD patterns of (A) single phase (Tio,36Alo.64)N layer and (B) multilayered TiNZ(Ti5Al)N coating with TiN and (Ti036Al064)N. The indexed peaks correspond to single phase (1) TiN, (2) (Ti9Al)N and 25 (3) cemented carbide. Similar to the results in fig 4, all deposited coatings summarized in tab 1 reveal single-phase cubic TiN and (Ti5Al)N structures. The residual stresses, σ, of the TiN and (Ti i-x Alx)N layers of the coating were evaluated by XRD measurements (see tab 1 ) using the sin2ψ method. The measurements were performed using CuKα-radiation on the TiN 220- and the (Ti i-x Alx)N 220- reflections, respectively. Stress values for layers thinner than <4 nm could not be deduced. The goniometer setup is shown in Fig. 5. Data was obtained using the side- inclination technique (ψ-geometry) with 11 , ψ-angles (positive and negative), equidistant within a sin2ψ range of 0 to 0.82 (ψ~65°). The residual stress values were evaluated using a Possion's ratio of v=0.25 and Young's modulus of E=450 GPa.
The total average composition of the coatings was estimated by energy dispersive spectroscopy (EDS) analysis area using a LEO Ultra 55 scanning electron microscope with a Thermo Noran EDS detector operating at 10 kV. The data were evaluated using a Noran System Six (NSS ver 2) software (see tab 1). Tab l
Figure imgf000009_0001
Example 2
Example 1 was repeated but using a pure Ta cathode (63mm in diameter, position (2b) in fig 2a) for growth of the TaN layers.
The total average composition of the coatings was estimated by energy dispersive spectroscopy (EDS) analysis (see example 1) and summarized in tab 2.
Tab 2
Figure imgf000010_0001
Example 3
Example 1 was repeated but using a Ti/Nb (95at%Ti + 5at% Nb) cathode (63 mm in diameter, position (2b) in fig 2a) for growth of the (Ti5Nb)N layers.
The total average composition of the coatings was estimated by energy dispersive spectroscopy (EDS) analysis (see example 1) and summarized in tab 3. Tab 3 d(T!,Nb)N d(TI,AI)N λ N Total coating Nb Ti Al N
Sample (nm) (nm) (nm) thickness (μm) (at%) (at%) (at%) (at%)
(Ti1AI)N 2,9 18,3 31 ,7 50,0
(Ti1Nb)N 3,0 2,3 47,7 50,0
25 1 ,0 4,1 5,1 608 3,1 0,5 23,8 25,7 50,0
26 2,5 2,6 5,1 569 2,9 1,1 32,6 16,3 50,0
J 27 4,1 1 ,1 5,2 558 2,9 1.8 41 ,4 6,8 50,0
£. 28 2,2 8,2 10,4 288 3,0 0,5 24,3 25,2 50,0
< 29 5,1 5,0 10,1 287 2,9 1 ,2 33,0 15,8 50,0 t 30 7,9 1 ,9 9,8 306 3,0 1 ,9 41 ,9 6,2 50,0
Z 31 4,1 16,0 20,1 134 2,7 0,5 24,1 25,5 50,0
§ 32 10,1 9,8 19,9 156 3,1 1 ,2 33,1 15,8 50,0
P 33 16,2 3,9 20,1 144 2,9 1 ,9 41,9 6,2 50,0
"1 34 9,9 40,1 50,0 62 3,1 0,5 23,9 25,7 50,0
35 25,0 24,9 49,9 60 3,0 1,2 32,9 16,0 50,0
36 39,6 10,1 49,7 56 2,8 1,8 41,7 6,5 50,0
Example 4
Example 1 was repeated but using a pure Nb cathode (63 mm in diameter, position (2b) in fig 2a) for growth of the NbN layers.
The total average composition of the coatings was estimated by energy dispersive spectroscopy (EDS) analysis (see example 1) and summarized in tab 4. Tab 4
Figure imgf000011_0001
Example 5
Example 1 was repeated but using a pure Zr cathode (63mm in diameter, position (2b) in fig 2a) for growth of the ZrN layers.
The total average composition of the coatings was estimated by energy dispersive spectroscopy (EDS) analysis (see example 1) and summarized in tab 5.
Tab 5
Figure imgf000012_0001
Example 6
Example 2 was repeated but using a pure V cathode (63 mm in diameter, position (2b) in fig 2a) for growth of the VN layers.
The total average composition of the coatings was estimated by energy dispersive spectroscopy (EDS) analysis (see example 1) and summarized in tab 6. Tab 6
Figure imgf000013_0001
Example 7
Example 2 was repeated but using a Al/Ti (95at%Al + 5at% Ti) cathode (63mm in diameter, position (2b) in fig 2a) for growth of the (Al5Ti)N layers.
The total average composition of the coatings was estimated by energy dispersive spectroscopy (EDS) analysis (see example 1) and summarized in tab 7.
Tab 7 d(T1,AI)N-L1 d(Ti,AI)N-L2 λ N Total coating Ti Al N
Sample (nm) (nm) (nm) thickness (μm) (at%) (at%) (at%)
(Ti1AI)N-LI 2,9 18,3 31 ,7 50,0 (Ti,AI)N-L2 3,2 46,4 3,6 49,8
73 1,0 3,9 4,9 633 3,1 23,8 26,2 50,0 -J 74 2,5 2,6 5,1 569 2,9 31,9 18,2 49,9 5 75 4,0 0,8 4,8 604 2,9 41,7 8,5 49,8
5. 76 2,1 8,1 10,2 294 3,0 23,8 26,2 50,0 < 77 5,1 4,9 10,0 290 2,9 32,5 17,6 49,9 B 78 8,1 1,8 9,9 303 3,0 41 ,2 8,9 49,8
3 79 3,9 15,8 19,7 137 2,7 23,6 26,4 50,0 Z 80 9,9 11 ,0 20,9 148 3,1 31 ,5 18,6 49,9 5 81 15,9 4,2 20,1 144 2,9 40,5 9,7 49,8
JZ 82 10,1 39,8 49,9 62 3,1 23,7 26,3 50,0 5T 83 25,1 24,9 50,0 60 3,0 32,3 17,8 49,9 84 40,1 9,4 49,5 57 2,8 41 ,0 9,2 49,8
SUBSTITUTE SHEETT (RULE 26) Example 8
Inserts from example 1 were tested according to:
Geometry: CNMG120408-MF1
Application: Continuous turning
Work piece material: AISI 316L
Cutting speed: 230 m/min
Feed: 0, 15 mm/rev
Depth of cut: 1 mm
Tool life criteria, flank wear (vb) >0,3 mm Result of test Tab 8
Figure imgf000014_0001
Example 9
Inserts from example 1 were tested according to:
Geometry: CNMGl 20412-MR3
Application: Continuous turning
SUBS mUTE SHEET fRl Il r Mij 14
Work piece material : Inconel 718, Cutting speed: 90 m/min
Feed: 0,2 mm/rev
Depth of cut: 0,5 mm
Tool life criteria, flank wear (vb) >0,2 mm
Result of test Tab 9
Figure imgf000015_0001
Example 10
Inserts from example 5 were tested according to:
Geometry: CNMG120408-MF1 Application: Continuous turning
Work piece material: AISI 316L Cutting speed: 250 m/min Feed: 0, 15 mm/rev Depth of cut: 1 mm Tool life criteria, flank wear (vb) >0,3 mm
Result of test Tab 10
Figure imgf000016_0001
Example 11
A used insert from example 8 was studied in more detail by TEM including electron diffraction, STEM and EDS. Fig 6 (A) shows a STEM micrographs of the coating of sample 4 (Tab 1). The image shows TiN rich regions (brighter contrast) and AlN rich regions (darker contrast). This is further verified by the EDS mapping in (C) and (D) showing the EDS maps of Ti (bright areas show Ti rich regions) and Al (bright areas show Al rich regions), respectively. Further, the typical size of the Ti and Al rich regions is on the order of 5 nm. Selected area electron diffraction patterns (B) show coherency and cubic structure over the layered structure.
SUBSTITUTE SHEFT- (RnI P off

Claims

Claims
1. Cutting tool for machining by chip removal comprising a body of a hard alloy of cemented carbide, cermet, ceramics, cubic boron nitride based material or high speed steel and a hard and wear resistant coating characterised in that said coating comprises a polycrystalline laminar, multilayered structure of metal nitride compounds, in a repetitive form ...MeN/(Ti,.x Alx)N /MeN/(Ti1-xAlx)N/MeN/(Ti]-x Alχ)N/MeN/(Ti,. XA1X)N... of cubic structured (Tii-XA1X)N layers where 0.3 < x < 0.95, preferably 0.45 < x < 0.75 and cubic structured MeN layers where Me is one or more of the metal element Ti, Zr, Hf, V, Nb, Ta, Mo and Al with a repeat period, λ, that is essentially constant throughout the entire laminated structure having a total thickness between 0.5 and 20 μm, preferably 1 to 10 μm , a repeat period, λ, of 5 nm < λ< 20 nm, preferably 5 nm < λ< 10 nm and layer thickness relation of 1/10 < (dMeN /d(-π,Ai)N) < 1/3, where the thickness dMeN is larger than dMeN ≥l nm.
2. Cutting tool according to claim l characterisedin that Me is Ti.
3. Cutting tool according to claim 1 characterised in that Me is Zr.
4. Cutting tool according to claim 1 characterised in that Me is V.
5. Cutting tool according to claim 1 characterised in that Me is Nb.
6. Cutting tool according to claim 1 characterised in that Me is Ta.
7. Cutting tool according to claim 1 characterised in that Me is Al.
8. Cutting tool according to claim 1 characterised in that Me is two or more of the metal elements Ti, V, Nb or Al.
9. Cutting tool according to claim 1 characterised in that Me is two or more of the metal elements Zr, V, Nb or Ta.
10. Cutting tool according to claim l characterisedin that Me is two or more of the metal elements Ti, Zr, V or Nb.
11. Cutting tool according to claim 1 characterised in that Me is two or more of the metal elements Zr, V or Nb.
12. Cutting tool according to the preceding claims characterised in that the total thickness of the multilayer coating is 2-10μm.
13. Cutting tool according to the preceding claims characterised in that the MeN layer has a compressive stress level between -12.0 < σ(MeN) < -3.0 GPa, preferably between -12.0 < σ(MeN) < -8.0 GPa whereas the (Tii-XA1X)N layer has a stress level varying between -6.0 < σ((Tii-x Alx)N) < -0.5 GPa, preferably between -6.0 <σ((Ti,.xAlχ)N) < -3.0 GPa.
14. Cutting tool according to the preceding claims characterised in that the average composition of the MeN/(Tii-x Alx)N multilayer coating is 46 at% < Zr + Hf + V +Nb + Ta + Mo + Ti + AK 54 at%, preferably 48 at% < Zr + Hf + V +Nb + Ta + Mo + Ti + Al < 52 at% and balanced N.
15. Cutting tool according to the preceding claims characterised in that said coating has been deposited with PVD, preferably cathodic arc evaporation.
16. Cutting tool according to the preceding claims c h a r a c t e r i s e d in that said body is coated with an inner single- and/or multilayer coating of TiN, TiC, Ti(C,N) or (Ti5Al)N, preferably (Ti5Al)N and/or an outer single- and/or multilayer coating of TiN, TiC, Ti(C5N) or (Ti5Al)N, preferably (Ti5Al)N, to a total thickness 1 to 20 μm, preferably 1 to 10 μm and most preferably 2 to 7 μm according to prior art.
17. Method of making a cutting tool according to claim 1 c h a r a c t e r i s e d in that said layers have a repetitive form MeN/(Tii-xAlx)N/MeN/(Tii-xAlx)N/MeN/(Tii. xAlx)N/MeN/... where Me is one or more of the metal elements Ti5 Zr5 Hf, V, Nb, Ta, Mo and Al5 preferably Ti, V5 Nb5 Ta or Al5 said (Ti,.xAlx)N, 0.3 < x < 0.95, preferably 0.45 < x < 0.75 and MeN layers are cubic structured, grown by cathodic arc evaporation using pure and/or alloyed Ti+Al and Me cathodes to yield the desired layer composition, with an evaporation current between 50 A and 200 A5 in an Ar + N2 atmosphere, preferably in a pure N2 at a total pressure of 0.5 Pa to 9.0 Pa, preferably 1.5 Pa to 5.0 Pa, with a bias between -10 V and -300 V, preferably between -20 V and -100V and at a temperature between 350 0C and 700 0C, preferably between 400 0C and 650 0C.
18. Use of a cutting tool inserts according to preceding claims for machining of stainless steel and super alloys at cutting speeds of 50-400 m/min, preferably 75-300 m/min, with an average feed, per tooth in the case of milling, of 0.08-0.5 mm, preferably 0.1-0.4 mm depending on cutting speed and insert geometrSummary
The present invention relates to a cutting tool comprising a body of a hard alloy of cemented carbide, cermet, ceramics, cubic boron nitride based material or high speed steel and on which at least one of the functioning parts of the surface thereof, a hard and wear resistant coating is applied. The coating comprises a polycrystalline laminar, multilayered structure of metal nitride compounds, in a repetitive form ...MeN/(Tii. x Alx)N /MeN/(Ti1-xAlx)N/MeN/(Ti1-xAlx)N/MeN/(Ti LxAlx)N... of cubic structured (Ti1- XA1X)N layers where 0.3 < x < 0.95 and cubic structured MeN layers where Me is one or more of the metal element Ti, Zr, Hf, V, Nb, Ta, Mo and Al. The laminated structure has a repeat period, λ, of 5 nm < λ< 20 nm, a layer thickness relation of 1/10 < (dMeN /d(Ti,Ai)N) < 1/3 and a thickness dMeN ≥l nm that is essentially constant throughout its total thickness up to 20 μm. The coating hardens as a nanocomposite, adapting its strength during spinodal decomposition of (Tii-XA1X)N in cubic TiN and cubic AlN domains where the additional cubic structured MeN layers provides means for locking a predominantly overall cubic coating structure thus suppressing the hexagonal AlN phase formation leading to improved high temperature metal cutting properties.
PCT/SE2009/050185 2008-02-21 2009-02-19 Multilayered coated cutting tool WO2009105024A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP09711935.8A EP2247772B1 (en) 2008-02-21 2009-02-19 Multilayered coated cutting tool
CN200980106128.3A CN101952482B (en) 2008-02-21 2009-02-19 Multilayered coated cutting tool
US12/867,889 US8409696B2 (en) 2008-02-21 2009-02-19 Multilayered coated cutting tool

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE0800398-0 2008-02-21
SE0800398 2008-02-21

Publications (1)

Publication Number Publication Date
WO2009105024A1 true WO2009105024A1 (en) 2009-08-27

Family

ID=40985768

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/SE2009/050185 WO2009105024A1 (en) 2008-02-21 2009-02-19 Multilayered coated cutting tool

Country Status (5)

Country Link
US (1) US8409696B2 (en)
EP (1) EP2247772B1 (en)
KR (1) KR20100116682A (en)
CN (1) CN101952482B (en)
WO (1) WO2009105024A1 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014037104A1 (en) 2012-09-08 2014-03-13 Oerlikon Trading Ag, Trübbach Ti-al-ta-based coating exhibiting enhanced thermal stability
CN104530793A (en) * 2014-12-13 2015-04-22 常熟市磊王合金工具有限公司 Wear-resistant polycrystalline diamond cutter
US9187648B2 (en) 2011-12-28 2015-11-17 Research Institute Of Industrial Science & Technology Hard coating layer and method for forming the same
WO2018215558A1 (en) 2017-05-23 2018-11-29 Oerlikon Surface Solutions Ag, Pfäffikon Thick TiAlTaN/AlCrN multilayer coating films on turbine components
EP4198169A1 (en) 2021-12-14 2023-06-21 CERATIZIT Austria Gesellschaft m.b.H. Cutting tool

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5783462B2 (en) * 2011-12-09 2015-09-24 三菱マテリアル株式会社 Surface coated cutting tool
KR101351843B1 (en) * 2012-05-02 2014-01-16 한국야금 주식회사 Hard coating film for cutting tools
KR101351844B1 (en) 2012-05-02 2014-01-16 한국야금 주식회사 Hard coating film for cutting tools
RU2495951C1 (en) * 2012-06-26 2013-10-20 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Ульяновский государственный технический университет" Method of producing sandwiched coating for cutting tool
RU2495953C1 (en) * 2012-07-03 2013-10-20 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Ульяновский государственный технический университет" Method of producing sandwiched coating for cutting tool
AR092945A1 (en) * 2012-10-10 2015-05-06 Oerlikon Trading Ag Trübbach COATING FOR HIGH TEMPERATURE USES WITH TRIBOLOGICAL REQUEST
US9103036B2 (en) * 2013-03-15 2015-08-11 Kennametal Inc. Hard coatings comprising cubic phase forming compositions
CN103143761B (en) * 2013-03-22 2015-06-24 武汉大学 AlTiN-MoN nano multi-layer composite coating milling cutter and preparation method thereof
JP6268530B2 (en) * 2013-04-01 2018-01-31 三菱マテリアル株式会社 Surface coated cutting tool with excellent chipping resistance due to hard coating layer
US9896767B2 (en) * 2013-08-16 2018-02-20 Kennametal Inc Low stress hard coatings and applications thereof
US9168664B2 (en) * 2013-08-16 2015-10-27 Kennametal Inc. Low stress hard coatings and applications thereof
US10023952B2 (en) * 2013-09-05 2018-07-17 Seco Tools Ab Coated cutting tool and a method for coating the cutting tool
JP6206800B2 (en) * 2013-09-05 2017-10-04 住友電工ハードメタル株式会社 Method for producing coating film
DE102014103220A1 (en) * 2014-03-11 2015-09-17 Walter Ag TiAIN layers with lamellar structure
JP6344601B2 (en) * 2014-06-17 2018-06-20 住友電工ハードメタル株式会社 Hard coating, cutting tool, and manufacturing method of hard coating
CN104152857B (en) * 2014-08-13 2017-05-17 徐州力泰钢结构有限公司 High-hardness TiAlZrN/CrN nano multi-layer coating and preparation method thereof
CN104260440B (en) * 2014-09-25 2016-06-15 温岭市温峤友德工具厂 A kind of nano-composite coating cutter containing aluminum titanium silicon yttrium nitrogen and preparation method thereof
US10669622B2 (en) * 2015-04-20 2020-06-02 Seco Tools Ab Coated cutting tool and a method for coating the cutting tool
JP6601692B2 (en) * 2015-08-03 2019-11-06 株式会社タンガロイ Coated cutting tool
US10837100B2 (en) * 2015-12-22 2020-11-17 Sandvik Intellectual Property Ab Method of producing a PVD layer and a coated cutting tool
US9994958B2 (en) 2016-01-20 2018-06-12 Sumitomo Electric Hardmetal Corp. Coating, cutting tool, and method of manufacturing coating
EP3436619B1 (en) * 2016-03-31 2022-04-20 Walter AG Coated cutting tool with h-aln and ti1-xalxcynz layers
JP6481897B2 (en) * 2016-09-16 2019-03-13 三菱マテリアル株式会社 Surface coated cutting tool
JP6701384B2 (en) * 2016-12-28 2020-05-27 住友電気工業株式会社 Film
EP3580368B1 (en) 2017-02-13 2023-11-22 Oerlikon Surface Solutions AG, Pfäffikon High temperature stable compositionally modulated hard coatings
US10570501B2 (en) 2017-05-31 2020-02-25 Kennametal Inc. Multilayer nitride hard coatings
WO2019065682A1 (en) * 2017-09-29 2019-04-04 三菱マテリアル株式会社 Surface-coated cutting tool in which hard coating layer exhibits exceptional chipping resistance
JP7063206B2 (en) * 2017-09-29 2022-05-17 三菱マテリアル株式会社 Surface coating cutting tool with excellent chipping resistance due to the hard coating layer
KR20210090227A (en) * 2018-11-09 2021-07-19 외를리콘 서피스 솔루션즈 아게, 페피콘 Cubic Al-rich AlTiN coating deposited from ceramic target
US20220297196A1 (en) * 2019-06-19 2022-09-22 Ab Sandvik Coromant Method of producing a coated cutting tool and a coated cutting tool
CN114196940B (en) * 2021-12-06 2023-04-28 赣州澳克泰工具技术有限公司 Composite coating cutter and preparation method and application thereof
DE102022113731A1 (en) * 2022-05-31 2023-11-30 Hartmetall-Werkzeugfabrik Paul Horn Gmbh Coated tool part and coating process

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06136514A (en) * 1992-10-26 1994-05-17 Kobe Steel Ltd Wear resistant multilayered hard coating film structure
US20020081161A1 (en) * 2000-10-31 2002-06-27 Mmc Kobelco Tool Co., Ltd. High-speed tool steel gear cutting tool and manufacturing method therefor
JP2002263941A (en) * 2001-03-14 2002-09-17 Mmc Kobelco Tool Kk Surface coated cemented carbide end mill with hard coating layer showing superior heat radiation
US20040026236A1 (en) * 2002-03-14 2004-02-12 Penich Ronald M. Nanolayered coated cutting tool and method for making the same

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5330853A (en) 1991-03-16 1994-07-19 Leybold Ag Multilayer Ti-Al-N coating for tools
DE69319531T2 (en) 1992-10-12 1999-04-15 Sumitomo Electric Industries Ultra thin film laminate
SE518145C2 (en) 1997-04-18 2002-09-03 Sandvik Ab Multilayer coated cutting tool
JP4185172B2 (en) 1997-06-19 2008-11-26 住友電工ハードメタル株式会社 Coated hard tool
CA2285460A1 (en) 1998-02-04 1999-08-12 Osg Corporation Hard multilayer coated tool having increased toughness
JP3031907B2 (en) 1998-03-16 2000-04-10 日立ツール株式会社 Multilayer coating member
US6743997B2 (en) * 2002-08-06 2004-06-01 Lear Corporation Rocker switch
SE526339C2 (en) 2002-09-04 2005-08-23 Seco Tools Ab Cut with durable refractory coating with composite structure
SE526338C2 (en) 2002-09-04 2005-08-23 Seco Tools Ab Cut with a hardened, hardened refractory coating

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06136514A (en) * 1992-10-26 1994-05-17 Kobe Steel Ltd Wear resistant multilayered hard coating film structure
US20020081161A1 (en) * 2000-10-31 2002-06-27 Mmc Kobelco Tool Co., Ltd. High-speed tool steel gear cutting tool and manufacturing method therefor
JP2002263941A (en) * 2001-03-14 2002-09-17 Mmc Kobelco Tool Kk Surface coated cemented carbide end mill with hard coating layer showing superior heat radiation
US20040026236A1 (en) * 2002-03-14 2004-02-12 Penich Ronald M. Nanolayered coated cutting tool and method for making the same

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Derwent World Patents Index; AN 1994-197526, XP003025193 *
DUCROS, C. ET AL.: "Multilayered and nanolayered hard nitride thin films deposited by cathodic arc evaporation. Part 1: Deposition, morphology and microstructure", SURFACE & COATINGS TECHNOLOGY, vol. 201, 2006, pages 136 - 142, XP005561272 *
DUCROS, C. ET AL.: "Multilayered and nanolayered hard nitride thin films deposited by cathodic arc evaporation. Part 2: Mechanical properties and cutting performances", SURFACE & COATINGS TECHNOLOGY, vol. 201, 2006, pages 1045 - 1052, XP005646896 *
See also references of EP2247772A4 *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9187648B2 (en) 2011-12-28 2015-11-17 Research Institute Of Industrial Science & Technology Hard coating layer and method for forming the same
WO2014037104A1 (en) 2012-09-08 2014-03-13 Oerlikon Trading Ag, Trübbach Ti-al-ta-based coating exhibiting enhanced thermal stability
DE102012017731A1 (en) 2012-09-08 2014-03-13 Oerlikon Trading Ag, Trübbach Ti-Al-Ta based coating with improved temperature resistance
US9506139B2 (en) 2012-09-08 2016-11-29 Oerlikon Surface Solutions Ag, Pfaffikon Ti—Al—Ta-based coating exhibiting enhanced thermal stability
CN104530793A (en) * 2014-12-13 2015-04-22 常熟市磊王合金工具有限公司 Wear-resistant polycrystalline diamond cutter
WO2018215558A1 (en) 2017-05-23 2018-11-29 Oerlikon Surface Solutions Ag, Pfäffikon Thick TiAlTaN/AlCrN multilayer coating films on turbine components
EP4198169A1 (en) 2021-12-14 2023-06-21 CERATIZIT Austria Gesellschaft m.b.H. Cutting tool
WO2023110293A1 (en) 2021-12-14 2023-06-22 Ceratizit Austria Gesellschaft M.B.H. Cutting tool

Also Published As

Publication number Publication date
US8409696B2 (en) 2013-04-02
EP2247772B1 (en) 2016-06-29
EP2247772A1 (en) 2010-11-10
CN101952482B (en) 2014-05-28
EP2247772A4 (en) 2015-07-29
KR20100116682A (en) 2010-11-01
CN101952482A (en) 2011-01-19
US20110111197A1 (en) 2011-05-12

Similar Documents

Publication Publication Date Title
EP2247772B1 (en) Multilayered coated cutting tool
KR101831014B1 (en) Coated cutting tool insert
KR101764101B1 (en) Nanolaminated coated cutting tool
EP2098611B1 (en) Layered coated cutting tool
US9540722B2 (en) Body with a metal based nitride layer and a method for coating the body
JP5654562B2 (en) Coated cutting tools for metal cutting applications that produce high temperatures
KR101492677B1 (en) Coated cutting tool for metal cutting applications generating high temperatures
EP2141257B1 (en) Oxide coated cutting insert and cathodic arc deposition associated
EP2636764A1 (en) Nanolaminated coated cutting tool
US10669622B2 (en) Coated cutting tool and a method for coating the cutting tool
WO2009110829A1 (en) Thermally stabilized (ti, si)n layer for cutting tool insert
CN109311099A (en) Surface-coated cutting tool
EP2262923B1 (en) Oxide coated cutting insert
KR20100126357A (en) Oxide coated cutting insert
CN111032913B (en) Coated cutting tool and method of coating the same

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200980106128.3

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 09711935

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2009711935

Country of ref document: EP

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 20107021176

Country of ref document: KR

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 12867889

Country of ref document: US